WITHDRAWN:46 XX Ovotesticular DSD with GNRHR, autosomal recessive heterozygous missens mutation and autosomal dominant heterozigous missense mutation of the PROKR2 gene, a case report.
Why is this work in the frame?
A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.
Post-publication record
OpenAlex flags this work as retracted, but it carries no matching Retraction Watch record in this frame.
Machine scores (provisional)
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
- Teacher spread
- 0.258 · how far apart the two teachers sit on this one work
- Validation status
score_only:v0-immature-baseline· verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it
Abstract
No abstract. This is not a gap in this database — OpenAlex has none either. 23.3% of the frame is in this state, and the screen finds HALF as much metaresearch here, so the absence is a measured bias rather than a missing field.
The record
- Venue
- Global Medical Genetics
- Topic
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Field
- Biochemistry, Genetics and Molecular Biology
- Canadian institutions
- National Association of Friendship Centres
- Funders
- —
- Keywords
- Missense mutationGeneticsMutationHeterozygote advantageBiologyGeneGenotype
- Has abstract in OpenAlex
- no